US12070479B1ActiveUtility
Decarboxylated cannabis compositions and methods of making the same
Est. expiryApr 19, 2041(~14.8 yrs left)· nominal 20-yr term from priority
A61K 36/3482A61K 2236/37B01D 5/006B01J 6/008A61K 31/352A61K 31/05A61K 36/185A61K 31/658
57
PatentIndex Score
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Cited by
11
References
20
Claims
Abstract
Decarboxylated cannabis compositions and methods of making and using the same are provided. The methods produce a decarboxylated product that has more terpenes and cannabidiol preserved and less oxidation of tetrahydrocannabinol to cannabinol, compared to a decarboxylated product made by a traditional decarboxylation process.
Claims
exact text as granted — not AI-modifiedWhat is claimed:
1. A method for preparing a decarboxylated cannabis composition, comprising:
(a) adding cannabis material to a reaction chamber,
(b) treating the reaction chamber with inert gas,
(c) sealing the reaction chamber,
(d) initiating a decarboxylation reaction of the cannabis material at about 70° C. to about 150° C., for about 0.5 hour to about 10 hours in the sealed reaction chamber,
(e) condensing within the sealed reaction chamber at about 0° C. to about 20° C.,
(f) retaining a decarboxylated cannabis composition within the sealed reaction chamber,
(g) optionally, storing the sealed reaction chamber comprising the decarboxylated cannabis composition at a temperature of about −40° C. to about −20° C., and
(h) unsealing the sealed reaction chamber to form an unsealed reaction chamber comprising the decarboxylated cannabis composition,
wherein no or substantially no solvent is added to the reaction chamber, and
wherein no by-products are removed from the reaction chamber prior to the unsealing of the sealed reaction chamber.
2. The method of claim 1 , wherein after step (h), the unsealed reaction chamber is placed in a water bath and heated to a temperature of about 50° C. to about 80° C. or 65° C. to about 75° C.
3. The method of claim 1 , further comprising filling a syringe or pipette with an amount of decarboxylated cannabis composition,
wherein the syringe or pipette is heated to a temperature of about 55° C. to about 75° C. or about 60° C. to about 70° C. prior to filling, and
wherein the filled syringed or pipette is maintained at a temperature of about 55° C. to about 75° C. or about 60° C. to about 70° C.
4. The method of claim 3 , wherein the syringe or pipette is a borosilicate glass syringe or borosilicate glass pipette.
5. The method of any of claim 3 , further comprising transferring the contents of the filled syringe or pipette into a vaporizer or vaporizer cartridge.
6. The method of claim 1 , wherein after step (c), the reaction chamber remains sealed until step (h).
7. The method of claim 1 , wherein the reaction chamber does not contain a filter or coils.
8. The method of claim 1 , further comprising placing an amount of the decarboxylated cannabis composition into a vaporizer or a vaporizer cartridge.
9. The method of claim 8 , wherein no solvents or additives are added to the decarboxylated cannabis composition prior to placing in a vaporizer or a vaporizer cartridge.
10. The method of claim 9 , wherein no flavoring agents are added to the decarboxylated cannabis composition prior to placing in a vaporizer or a vaporizer cartridge.
11. The method of claim 1 , wherein the cannabis material comprises a cannabis extract, a cannabis concentrate, dried or live plant matter, or a mixture thereof.
12. The method of claim 1 , wherein the cannabis material comprises no or substantially no solvent.
13. The method of claim 1 , wherein the inert gas comprises nitrogen or argon gas.
14. The method of claim 1 , wherein the reaction chamber is a glass vessel.
15. The method of claim 1 , wherein step (d) occurs at about 90° C. to about 130° C. or about 110° C. to about 125° C.
16. The method of claim 1 , wherein step (d) occurs for about 1 to about 5 hours or about 2 to about 3 hours.
17. The method of claim 1 , wherein the decarboxylated cannabis composition comprises no additives and substantially no tetrahydrocannabinolic acid (THCA), cannabidiolic acid (CBDA), or cannabigerolic acid (CBGA).
18. The method of claim 1 , further comprising (g) storing the sealed reaction chamber comprising the decarboxylated cannabis composition at a temperature of about −40° C. to about −20° C.
19. The method of claim 18 , wherein after step (g), the sealed reaction chamber is placed in a water bath and heated to a temperature of about 50° C. to about 80° C. or about 65° C. to about 75° C.
20. The method of claim 3 , wherein the syringe or pipette is made from glass, porcelain, or steel.Cited by (0)
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